Variant #0000311476 (NC_000002.11:g.27601346G>A, NM_144631.5:c.787C>T (ZNF513))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.27601346G>A
DNA change (hg38) g.27378479G>A
Published as ZNF513(NM_144631.6):c.787C>T (p.R263W)
ISCN -
DB-ID ZNF513_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNX17 NM_014748.3 ?/. - c.*1760G>A r.(=) p.(=)
ZNF513 NM_144631.5 ?/. - c.787C>T r.(?) p.(Arg263Trp)
PPM1G NM_177983.2 ?/. - c.*3120C>T r.(=) p.(=)


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